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Loratidine Tablet

NAFDAC Reg. Rárá. B4-0483 · Oògùn

Forukọsilẹ pẹlu NAFDAC. Iforukọsilẹ ti nṣiṣe lọwọAs of 6 November 2026 · synced automatically from official sources.
Ọja
Loratidine Tablet
Nọmba NAFDAC
B4-0483
Ohun elo ti nṣiṣe lọwọ
Loratadine
Agbara
10 mg
Fọọmu
Tablet
Iwọn iṣakojọpọ
10 x 10's
Olupese
Ko ṣe atokọ
Olubẹwẹ (oluranlowo)
Azmu Pharmaceuticals Limited
Ti fọwọsi
24 Jun 2021
Ipò
Inactive Wo lórí NAFDAC ↗
Iforukọsilẹ wulo si
23 Jun 2026
Tani o ṣe itaniji
Kosi ikankan ti a rii.
Ijabọ Agbegbe
Kò sí
Àwọn àyẹ̀wò àsìkò
0

Nipa oogun naa: Loratadine: uses, dosage and brands worldwide

What we found

  • Loratidine Tablet is on the NAFDAC register with an active registration (B4-0483). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Loratidine Tablet

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Tani o jẹ fun

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes • sneezing • itching of the nose or throat

Bii o ṣe le mu u ati igba melo ni
  • Adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours
  • Children under 6 years of age
  • Ask a doctor consumers with liver or kidney disease
  • Ask a doctor
While you are taking it
  • Do not take more than directed
  • Taking more than directed may cause drowsiness
Talk to a doctor first if
  • Liver or kidney disease
  • Your doctor should determine if you need a different dose
Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed. Taking more than directed may cause drowsiness. Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Àbájáde tí ó ṣeéṣe

An allergic reaction to this product occurs. Seek medical help right away.

Pregnancy and breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

How to store it

• do not use if printed foil under cap is broken or missing • store between 20 ° to 25 ° C (68 ° to 77 ° F) Keep out of reach of children.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2026-02-25.

Label for loratadine, the active ingredient registered with NAFDAC.

Check your pack of Loratidine Tablet

Add the expiry date on your pack for a full Trust Score.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Loratidine Tablet

What is in Loratidine Tablet?

Loratidine Tablet contains Loratadine (10 mg), as tablet, according to its NAFDAC registration record.

Is Loratidine Tablet registered with NAFDAC?

Yes. Loratidine Tablet is listed on the NAFDAC register under registration number B4-0483, and its registration is active as of 6 November 2026.

Has Loratidine Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Loratidine Tablet in our automatically synced alert list.

How can I check that my pack of Loratidine Tablet is genuine?

Run a free authenticity scan with the NAFDAC number B4-0483, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Loratidine Tablet?

Follow your prescription or the leaflet in your pack. The official label says: adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor…

What is Loratidine Tablet used for?

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes • sneezing • itching of the nose or throat (Summarised from the official U.S. FDA label for loratadine. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.